This is the largest of the research cores, consisting of nine investigators working on various aspects of mutagenesis and carcinogenesis. It brings together toxicologists, molecular biologists, epidemiologist and geneticists. The multi-disciplinary projects range in scope from studies on DNA damage through human population studies on biomarkers and cancer risk. The core leader is Dr. Allan Smith. Accomplishments from his laboratory include evidence for genotoxic effects in exfoliated bladder epithelial cells in human population exposed to arsenic in drinking water. Other accomplishments of this core include findings by Dr. Ames that oxidative DNA damage plays a major role in aging and cancer, that mitochondria are an important source of these oxidants, and that dietary antioxidant can protect against oxidative damage in humans. New Salmonella tester strains (Ames II test) have also been developed. New fluorescent labels for analysis of nucleic acid have been developed by Dr. Alexander Glazer. Dr. Lois Gold, in collaboration with Dr. Bruce Ames, has developed ranking schemes and databases for carcinogenic agents to which humans are exposed. Dr. Alexander Karu has developed immunoassays to detect PCBs and PAHs. Dr. Stuart Linn has added to our knowledge of the steps involved in oxidative DNA damage. Dr. Martyn Smith has new findings on the genotoxic effects of benzene metabolites, as well as development of a FISH technique for micronuclei in exfoliated bladder experiments which was used in the studies of Dr. Allan Smith.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
5P30ES001896-24
Application #
6587605
Study Section
Project Start
2002-04-01
Project End
2003-03-31
Budget Start
Budget End
Support Year
24
Fiscal Year
2002
Total Cost
$228,547
Indirect Cost
Name
University of California Berkeley
Department
Type
DUNS #
094878337
City
Berkeley
State
CA
Country
United States
Zip Code
94704
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Ren, Xuefeng; Lim, Sophia; Ji, Zhiying et al. (2011) Comparison of proliferation and genomic instability responses to WRN silencing in hematopoietic HL60 and TK6 cells. PLoS One 6:e14546

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